ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

Antibacterial Hand wipes by

Drug Labeling and Warnings

Antibacterial Hand wipes by is a Otc medication manufactured, distributed, or labeled by MY IMPORTS USA LLC, Kangna (Zhejiang) Medical Supplies Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

.Antibacterial

USE

decreases bacteria on skin

Warning

For external use only.
Do not use if you are allergic to any of theingredients.
When using this product do not get into eyes.
f contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rashdevelops and continues for more than 72 hours

Keep out of reach of children. lf swallowedget medical help or contact a Poison ControlCenter right away.

Directions

Adults and children 2 years and over.Apply to hands and allow to dry without wiping.
Children under 2 years. Ask a doctorbefore use.

Inactive ingredients

Water, Glycerin, Phenoxyethanol, SodiumBenzoate, Cocamidopropyl PG-DimoniumChloride Phosphate, Disodium EDTA, Polysorbate20, Citric Acid, Ethylhexylglycerin, AloeBarbadensis Leaf Juice, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-9999
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID (UNII: 2968PHW8QP)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-9999-1	25 in 1 CONTAINER	01/15/2025
1		0.12 g in 1 BAG; Type 0: Not a Combination Product
2	NDC: 51628-9999-2	25 in 1 PAIL	01/15/2025
2		0.12 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 51628-9999-3	80 in 1 PAIL	08/18/2025
3		0.4 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/15/2025

Labeler - MY IMPORTS USA LLC (195767988)

Establishment
Name	Address	ID/FEI	Business Operations
Kangna (Zhejiang) Medical Supplies Co., Ltd.		554530173	manufacture(51628-9999)